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| Term | platelet-type bleeding disorder 9 | ID (Ontology) | DOID:0111045 (Human Disease) |
| Definition | A blood platelet disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has_material_basis_in mutation in the ITGA2 gene on chromosome 5q11.2. | ||
| Also Known As | "BDPLT9" ; "collagen platelet receptor deficiency" ; "glycoprotein Ia deficiency" (for all, see Synonyms field below) | ||
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autosomal genetic disease |__autosomal dominant disease__ blood coagulation disease | |__blood platelet disease______| platelet-type bleeding disorder 9 |
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autosomal dominant disease blood platelet disease |
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ICD10CM:D69.8 MIM:614200 ORDO:98886 |
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